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प्रश्न
In which of the following molecules carbon atom marked with asterisk (*) is asymmetric?
(a) \[\begin{array}{cc}
\ce{H}\\
|\\
\phantom{.}\ce{C^*}\phantom{}\\
\phantom{}/\phantom{..}|\phantom{..}\backslash\phantom{}\\
\phantom{.}\ce{I}\phantom{...}\ce{Br}\phantom{..}\ce{Cl}
\end{array}\]
(b) \[\begin{array}{cc}
\ce{D}\\
|\\
\phantom{.}\ce{C^*}\phantom{}\\
\phantom{}/\phantom{..}|\phantom{..}\backslash\phantom{}\\
\phantom{.}\ce{I}\phantom{...}\ce{Br}\phantom{..}\ce{Cl}
\end{array}\]
(c) \[\begin{array}{cc}
\ce{H}\\
|\\
\phantom{.}\ce{C^*}\phantom{}\\
\phantom{}/\phantom{..}|\phantom{..}\backslash\phantom{}\\
\phantom{..}\ce{OH}\phantom{..}\ce{C2H5}\phantom{}\ce{CH3}
\end{array}\]
(d) \[\begin{array}{cc}
\ce{H}\\
|\\
\phantom{.}\ce{C^*}\phantom{}\\
\phantom{}/\phantom{..}|\phantom{..}\backslash\phantom{}\\
\phantom{..}\ce{H}\phantom{...}\ce{C2H5}\phantom{}\ce{CH3}
\end{array}\]
विकल्प
(a), (b), (c), (d)
(a), (b), (c)
(b), (c), (d)
(a), (c), (d)
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उत्तर
(a), (b), (c)
Explanation:
Asymmetric/chiral carbon atom is that in which all of its four valencies with four different groups or atoms.
In molecules (a), (b) and (c), all have asymmetric carbon as each carbon has satisfied all four valencies with four different groups or atoms.
In molecule (d), carbon satisfies two of its valencies with two hydrogen atoms i.e., similar atom. So, it is not an asymmetric carbon atom.
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संबंधित प्रश्न
Draw the structure of major monohalo products in the following reaction:

Draw the structure of major monohalo products in the following reaction:

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:
(CH3)3CCH2CH(Br)C6H5
Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:
CH3C(C2H5)2CH2Br
Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:
CH3C(Cl)(C2H5)CH2CH3
Which of the following is an example of vic-dihalide?
Which is the correct IUPAC name for \[\begin{array}{cc}
\ce{CH3 - CH - CH2 - Br}\\
\phantom{}|\phantom{.......}\\
\phantom{}\ce{C2H5}\phantom{....}
\end{array}\]?
Haloalkanes contain halogen atom (s) attached to the sp3 hybridised carbon atom of an alkyl group. Identify haloalkane from the following compounds.
(i) 2-Bromopentane
(ii) Vinyl chloride (chloroethene)
(iii) 2-chloroacetophenone
(iv) Trichloromethane
Why can aryl halides not be prepared by reaction of phenol with \[\ce{HCl}\] in the presence of \[\ce{ZnCl2}\]?
Match the items of Column I and Column II.
| Column I | Column II | |
| (i) | SN1 reaction | (a) vic-dibromides |
| (ii) | Chemicals in fire extinguisher | (b) gem-dihalides |
| (iii) | Bromination of alkenes | (c) Racemisation |
| (iv) | Alkylidene halides | (d) Saytzeff rule |
| (v) | Elimination of HX from alkylhalide | (e) Chlorobromocarbons |
Classify the following compound as a primary, secondary and tertiary halide.
1-Bromobut-2-ene
Classify the following compound as a primary, secondary and tertiary halide.
4-Bromopent-2-ene
Name the following halide according to the IUPAC system and classify it as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:
\[\ce{CH_3CH_2C(CH_3)_2CH_2I}\]
Name the following halide according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3C(Cl)(C2H5)CH2CH3}\]
Name the following halide according to IUPAC system and classify as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
CH3CH2C(CH3)2CH2l
Name the following halides according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3C(C2H5)2CH2Br}\]
Name the following halide according to IUPAC system and classify as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3C(C2H5)2CH2Br}\]
Write the structure of the following organic halogen compound.
4-tert-Butyl-3-iodoheptane
Draw the structure of major monohalo products in the following reaction:

